HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047157Generated: October 31, 2026
Hydrochloric Acid → (S)-ethyl 6-bromo-1-(1-(tert-butoxycarbonyl)piperidin-3-yl)-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylate
https://huagongshe.com/reaction/1047157
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-butyl (3S)-3-aminopiperidine-1-carboxylate | HCID 1501975 | — |
| Reactant | Ethyl 2-(5-bromo-2-fluoronicotinoyl)-3-(dimethylamino)acrylate | HCID 68749333 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (S)-ethyl 6-bromo-1-(1-(tert-butoxycarbonyl)piperidin-3-yl)-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylate | HCID 68796045 | 75.5% |
Reaction Steps
Ethyl 2-(5-bromo-2-fluoronicotinoyl)-3-(dimethylamino)acrylate (Intermediate 3, 2.0 g, 5.79 mmol), (S)-tert-butyl 3-aminopiperidine-1-carboxylate (1.160 g, 5.79 mmol), and potassium carbonate (2.042 g, 7.38 mmol) were combined in DMF (10.0 mL). The reaction mixture was heated at 90° C. for 2 h. The reaction mixture was cooled to 0° C. and 1N HCl was slowly added until pH was 5. The resulting precipitate was collected by filtration, washed with water and dried overnight to yield a light yellow solid (2.10 g, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569484B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-a2847f7ada994500b35207c8fa8ab258 |
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| Source note | uspto-grants-2013_10 |
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